174006-70-3 Usage
General Description
The chemical 2-[4-(trifluoromethyl)phenyl]-1,3-thiazole-4-carbaldehyde, also known as Thiazole-4-carbaldehyde, is a compound with the molecular formula C10H6F3NO S. It is a yellow liquid with a molecular weight of 239.22 g/mol. This chemical is commonly used as an intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. It is also used as a building block for the production of various dyes and pigments. Thiazole-4-carbaldehyde has potential applications in the field of medicinal and pharmaceutical chemistry, particularly in the development of new drugs. It is important to handle this chemical with care due to its potential hazardous properties.
Check Digit Verification of cas no
The CAS Registry Mumber 174006-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,0,0 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 174006-70:
(8*1)+(7*7)+(6*4)+(5*0)+(4*0)+(3*6)+(2*7)+(1*0)=113
113 % 10 = 3
So 174006-70-3 is a valid CAS Registry Number.
174006-70-3Relevant articles and documents
Metal-Free Aerobic Oxidative Selective C-C Bond Cleavage in Heteroaryl-Containing Primary and Secondary Alcohols
Xia, Anjie,Qi, Xueyu,Mao, Xin,Wu, Xiaoai,Yang, Xin,Zhang, Rong,Xiang, Zhiyu,Lian, Zhong,Chen, Yingchun,Yang, Shengyong
supporting information, (2019/05/07)
A transition-metal-free aerobic oxidative selective C-C bond-cleavage reaction in primary and secondary heteroaryl alcohols is reported. This reaction was highly efficient and tolerated various heteroaryl alcohols, generating a carboxylic acid derivative and a neutral heteroaromatic compound. Experimental studies combined with density functional theory calculations revealed the mechanism underlying the selective C-C bond cleavage. This strategy also provides an alternative simple approach to carboxylation reaction.
